23
Participants
Start Date
June 30, 2008
Primary Completion Date
August 31, 2011
Study Completion Date
August 31, 2012
mapatumumab
3, 10, or 30 mg/kg IV (in the vein), on day 1 of each 21 day cycle
sorafenib
400 mg orally, twice a day continuously in each cycle
University of Pennsylvania- Abramson Cancer Center, Philadelphia
UNC Lineberger Comprehensive Cancer Center, Chapel Hill
University of Florida, Gainesville
Mayo Clinic, Rochester
University of Colorado Cancer Center, Aurora
Cedars-Sinai Health System, Los Angeles
Collaborators (1)
GlaxoSmithKline
INDUSTRY
Human Genome Sciences Inc., a GSK Company
INDUSTRY